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Gemini GEM3136

by Medline Industries, Inc.

Gemini GEM3136 is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 14 Oct 2016 (UDI-DI 20080196921345), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number20080196921345 UDI-DI Date14 Oct 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Gemini
Generic name
Sterilization packaging, single-use
Model / Ref / Catalog
GEM3136
Primary DI / UDI-DI
20080196921345
FDA product code
FRG
GMDN term
Sterilization packaging, single-use
Device class
Class II
Regulation number
880.6850
GUDID distribution status
In Commercial Distribution
Size
Length — 36 Inch
Width — 36 Inch

Related devices

Category: Sterilization packaging, single-use

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Single use
  • Over-the-counter
  • Lot / batch number
Other properties (12, all answered No)